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NGS for Cardiovascular



Comprehensive Arrhythmia NGS Panel

Title Phenotype Inheritance
ANK2 cardiac arrhythmia, ankyrin-b-related AD
ANK2 long qt syndrome 4 AD
NPPA atrial fibrillation, familial, 6 AD
NPPA atrial standstill 2 AR
CASQ2 ventricular tachycardia, catecholaminergic polymorphic, 2 AR
CACNA1C brugada syndrome 3  
CACNA1C long qt syndrome 8  
CACNA1C timothy syndrome AD
CALM1 long qt syndrome 14 AD
CALM1 ventricular tachycardia, catecholaminergic polymorphic, 4 AD
CALM2 long qt syndrome 15 AD
GJA5 atrial fibrillation, familial, 11 AD
GJA5 atrial standstill, digenic (gja5/scn5a) AD
DSG2 arrhythmogenic right ventricular dysplasia 10 AD
DSC2 arrhythmogenic right ventricular dysplasia 11 AD, AR
DSC2 arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair AD, AR
DSP arrhythmogenic right ventricular dysplasia 8 AD
KCNH2 long qt syndrome 2, acquired, susceptibility to AD
KCNH2 long qt syndrome 2 AD
KCNH2 short qt syndrome 1  
JUP arrhythmogenic right ventricular dysplasia 12 AD
JUP naxos disease AR
KCNA5 atrial fibrillation, familial, 7 AD
KCNE1 jervell and lange-nielsen syndrome 2 AR
KCNE1 long qt syndrome 5 AD
RYR2 arrhythmogenic right ventricular dysplasia 2 AD
RYR2 ventricular tachycardia, catecholaminergic polymorphic, 1 AD
TGFB3 arrhythmogenic right ventricular dysplasia 1 AD
TGFB3 loeys-dietz syndrome 5 AD
CACNB2 brugada syndrome 4  
SCN5A {sudden infant death syndrome, susceptibility to} AR
SCN5A atrial fibrillation, familial, 10 AD
SCN5A brugada syndrome 1 AD
SCN5A cardiomyopathy, dilated, 1e AD
SCN5A heart block, nonprogressive AD
SCN5A heart block, progressive, type ia AD
SCN5A long qt syndrome 3 AD
SCN5A sick sinus syndrome 1 AR
SCN5A ventricular fibrillation, familial, 1  
SCN1B atrial fibrillation, familial, 13 AD
SCN1B brugada syndrome 5  
SCN1B cardiac conduction defect, nonspecific  
KCNJ2 Andersen Tawil syndrome AD
KCNJ2 atrial fibrillation, familial, 9 AD
KCNJ2 short qt syndrome 3  
KCNJ5 long qt syndrome 13 AD
SNTA1 long qt syndrome 12 AD
CAV3 long qt syndrome 9 AD
SCN2B atrial fibrillation, familial, 14 AD
ABCC9 atrial fibrillation, familial, 12 AD
PRKAG2 wolff-parkinson-white syndrome AD
PKP2 arrhythmogenic right ventricular dysplasia 9 AD
TRDN ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness AR
KCNE2 atrial fibrillation, familial, 4  
KCNE2 long qt syndrome 6 AD
AKAP9 long qt syndrome 11 AD
KCNE3 brugada syndrome 6  
HCN4 brugada syndrome 8  
HCN4 sick sinus syndrome 2 AD
KCND3 brugada syndrome 9 AD
LDB3 left ventricular noncompaction 3 AD
TRPM4 progressive familial heart block, type ib AD
CTNNA3 arrhythmogenic right ventricular dysplasia, familial, 13 AD
SCN3B atrial fibrillation, familial, 16 AD
SCN3B brugada syndrome 7 AD
SCN4B atrial fibrillation, familial, 17 AD
SCN4B long qt syndrome 10 AD
KCNQ1 {long qt syndrome 1, acquired, susceptibility to} AD
KCNQ1 atrial fibrillation, familial, 3 AD
KCNQ1 jervell and lange-nielsen syndrome AR
KCNQ1 long qt syndrome 1 AD
KCNQ1 short qt syndrome 2 AD
GPD1L brugada syndrome 2  
TMEM43 arrhythmogenic right ventricular dysplasia 5 AD
CACNA2D1 Short QT syndrome AD
CALM3 Ventricular tachycardia, catecholaminergic polymorphic 6 AD
CALM3 Long QT syndrome 16 AD
KCNJ8 Brugada syndrome #N/A
KCNJ8 ventricular fibrillation with early repolarization #N/A